AI Article Synopsis

  • Matching for specific HLA alleles is essential for successful hematopoietic stem cell transplantation (HSCT), but HLA mismatches can increase the risk of complications like acute graft versus host disease (GvHD).
  • The study examined the impact of mismatches in a specific genomic region (gamma block) on HSCT outcomes in 51 patients, finding that 29.41% had GT-matched donor-recipient pairs.
  • While univariate analysis indicated that GT mismatches were linked to a higher risk of aGvHD, this was not confirmed in multivariate analysis, and the study's small sample size calls for more research to clarify these findings.

Article Abstract

Matching for HLA-A, -B, -C, -DRB1, -DQB1 alleles is the gold standard in hematopoietic stem cell transplantation (HSCT). However, this is often not enough to prevent postransplantational complications. The HLA mismatches (MM) have been associated with higher risk of acute graft versus host disease (GvHD). Gamma block (GB) is located in central HLA region, between HLA-B/C and HLA-DRB/DQB blocks and contains many inflammatory and immune regulatory genes. Single nucleotide polymorphisms (SNPs) within that block can be considered as markers for MHC haplotype matching. Aim of the research was to test whether MM in GB impact the outcome of HSCT in 51 patients transplanted with HLA 10/10 matched unrelated donor. The recipient-donor pairs were typed using PCR SSP kit that detects 25 SNPs within GB. Fifteen out of 51 (29.41%) pairs were GT matched (GT-M) while 36 out of 51 pairs (70.59%) were mismatched (GT-MM). In a univariate analysis, GT-MM was a significant risk factor associated with aGvHD (P = 0.041), although this association was not seen in multivariate analysis. No significant difference in overall survival and relapse occurrence was seen. These results were obtained on a small sample, and it is necessary to further test the possible role of GT matching in unrelated HSCT.

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Source
http://dx.doi.org/10.1016/j.humimm.2019.10.005DOI Listing

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